Variant #0000623308 (NC_000015.9:g.83328383_83328386dup, NM_004644.3:c.3178_3181dup (AP3B2))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.83328383_83328386dup
DNA change (hg38) g.82659631_82659634dup
Published as AP3B2(NM_001278512.1):c.3235_3238dupACTG (p.V1080Dfs*62)
ISCN -
DB-ID AP3B2_000009
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-06 17:36:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP3B2 NM_004644.3 +?/. - c.3178_3181dup r.(?) p.(Val1061AspfsTer62)


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